NCT06830447

Brief Summary

The test retest reliability of Myocene will be tested.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Mar 2025

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 5, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

February 17, 2025

Completed
12 days until next milestone

Study Start

First participant enrolled

March 1, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2025

Completed
Last Updated

February 17, 2025

Status Verified

February 1, 2025

Enrollment Period

1 month

First QC Date

February 5, 2025

Last Update Submit

February 11, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • low-frequency fatigue

    Low frequency fatigue will be assessed using myocene. Participants will seat on the device with their leg positioned against the "Myo-sensor". Electrical muscle stimulation will be applied using biphasic square waves with a pulse width of 400 µs, delivered through three electrodes. A pre-programmed Myocene protocol, which has a duration of about 2 minutes will be applied

    baseline and 30 minutes post baseline.

Study Arms (1)

Single group

participants will perform the myocene measurement twice

Other: low-frequency fatigue

Interventions

Low frequency fatigue tested with myocene

Single group

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Participants will be sports science students, physically active.

You may qualify if:

  • active individuals

You may not qualify if:

  • injured participants
  • unhealthy volunteers

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Fatigue

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 5, 2025

First Posted

February 17, 2025

Study Start

March 1, 2025

Primary Completion

April 1, 2025

Study Completion

May 1, 2025

Last Updated

February 17, 2025

Record last verified: 2025-02